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Efficacy and Safety of G Protein-Biased µ-Opioid Receptor Agonists in the Treatment of Moderate-to-Severe Pain Following Off-Pump Coronary Artery Bypass Grafting: A Randomized Blinded Study

Efficacy and Safety of G Protein-Biased µ-Opioid Receptor Agonists in the Treatment of Moderate-to-Severe Pain Following Off-Pump Coronary Artery Bypass Grafting: A Randomized Blinded Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500101524
Enrollment
Unknown
Registered
2025-04-25
Start date
2025-05-01
Completion date
Unknown
Last updated
2025-04-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coronary atherosclerotic heart disease

Interventions

Oliceridine group:Ten minutes before the end of the operation, a loading dose is first administered: The experimental group is intravenously injected with 1.5 mg of oliceridine. Twenty-four-hour patie
Sufentanil group:Ten minutes before the end of the operation, a loading dose is first administered: The control group is intravenously injected with 7.5 µg of sufentanil. Twenty-four-hour patient-cont

Sponsors

Qilu Hospital of Shandong University Dezhou Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic criteria for coronary heart disease in "Internal Medicine", and undergo OPCABG treatment for three-branch coronary artery lesions; 2. Have signed an informed consent form; 3. Age > = 60 years old.

Exclusion criteria

Exclusion criteria: 1. Those with severe liver and kidney organ dysfunction; 2. Patients with autoimmune diseases, cerebrovascular diseases and malignant tumors; 3. Those who use drugs that affect mental and nervous system activity.

Design outcomes

Primary

MeasureTime frame
The response rate to the experimental drug at each time point within 24 hours after the administration of the loading dose;

Secondary

MeasureTime frame
The response rate to the experimental drug at each time point within 1 hour after the administration of the loading dose;The rate of rescue analgesia within 24 hours after the administration of the loading dose;

Countries

China

Contacts

Public ContactSisi Wei

Qilu Hospital of Shandong University Dezhou Hospital

547931723@qq.com+86 150 9250 5663

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026